Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756155Generated: November 1, 2026

Potassium Fluoride → Ethyl 3-(3thienyl)phenoxyacetate

https://huagongshe.com/reaction/1756155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
ReactantEthyl 2-(3-bromophenoxy)acetateHCID 5197439—
ReactantStannane, tributyl-3-thienyl-HCID 10959689—
CatalystHCID 178418397HCID 178418397—
SolventO-XyleneHCID 7237—
ProductEthyl 3-(3thienyl)phenoxyacetateHCID 1991694064.6%

Reaction Steps

2.6 g of the resulting ether compound, 5.3 g of tri-n-butyl(3-thienyl)tin and 20 mg of tetrakis(triphenylphosphine)palladium were dissolved in 10 ml of xylene, and the mixture was refluxed for 5.5 hours. A 25% aqueous solution of potassium fluoride was added to the solution, and then the precipitate was removed by filtration. The organic layer separated was worked up in a customary manner, and the product was purified by silica gel column chromatography [hexane/ethyl acetate=20/1→15/1] to give 1.7 g of ethyl 3-(3thienyl)phenoxyacetate as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05439932
Source datasetuspto-grants-1995_08
ORD IDord-f7b35241cf3940bdb8f07315907b7130
Source noteuspto-grants-1995_08